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3-Methylglutaconic aciduria

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3-Methylglutaconic aciduria (MGA) is used to describe at least five disorders that impair the body's ability to make energy in the mitochondria. [1]

8 relations: Barth syndrome, List of diseases (0–9), List of disorders included in newborn screening programs, List of OMIM disorder codes, OPA3, SERAC1, Tafazzin, 3-Methylglutaconic acid.

Barth syndrome (BTHS), also known as 3-Methylglutaconic aciduria type II, is an X-linked genetic disorder.

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The List of diseases starting with a non-letter is part of the complete list of diseases.

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This is a list of disorders included in newborn screening programs around the world, along with information on testing methodologies, disease incidence and rationale for being included in screening programs.

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This is a list of disorder codes in the Online Mendelian Inheritance in Man (OMIM) database.

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Optic atrophy 3 protein is a protein that in humans is encoded by the OPA3 gene.

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Serine active site containing 1 is a protein in humans that is encoded by the SERAC1 gene.

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Tafazzin is a protein that in humans is encoded by the TAZ gene.

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3-Methylglutaconic acid is a glutarate which builds up in the urine in 3-methylglutaconic aciduria or 3-hydroxy-3-methylglutaric aciduria.

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Redirects here:

3 methylglutaconyl coa hydratase deficiency, 3-Methylglutaconic acidemia, 3-Methylglutaconic aciduria type 1, 3-Methylglutaconic aciduria type 3, 3-Methylglutaconic aciduria type 4, 3-Methylglutaconic aciduria type 5, 3-Methylglutaconic aciduria type I, 3-Methylglutaconic aciduria type III, 3-Methylglutaconic aciduria type IV, 3-Methylglutaconic aciduria type V, 3-Methylglutaconyl-CoA Hydratase Deficiency, 3-methyl glutaconic aciduria, 3-methylglutaconic aciduria, 3MGA, Costeff syndrome, MGA type 1, MGA type 3, MGA type 4, MGA type 5, MGA type I, MGA type III, MGA type IV, MGA type V.

References

[1] https://en.wikipedia.org/wiki/3-Methylglutaconic_aciduria

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